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Hallervorden-Spatz syndrome: Difference between revisions
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[https://www.wikigenes.org/e/mesh/e/9516.html wikigenes:Hallervorden-Spatz Syndrome] | [https://www.wikigenes.org/e/mesh/e/9516.html wikigenes:Hallervorden-Spatz Syndrome] | ||
[https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4892321/pdf/BCN-7-165.pdf Case Report: Hallervorden–Spatz Syndrome with Seizures] | |||
<references/> | <references/> | ||
[[nl:Syndroom van Hallervorden-Spatz]] | [[nl:Syndroom van Hallervorden-Spatz]] | ||
Revision as of 19:18, 20 June 2017
Hallervorden-Spatz syndrome, now known as pantothenate kinase-associated neurodegeneration (PKAN), is an autosomal recessive disorder causing involuntary spasticity and progressive dementia [1]
Disease classification WHO
G 23.0 Hallervorden-Spatz syndrome
Links
wikigenes:Hallervorden-Spatz Syndrome
Case Report: Hallervorden–Spatz Syndrome with Seizures
read Panthothenate kinase-associated neurodegeration Interwiki via Wikidata